Canonical Allele Identifier: CA016047

Gene: FBN1

Linked Data

• ClinVar Variation Id: 155794
• ClinVar RCV Id: RCV000143894
• dbSNP Id: rs587782947
• MyVariant Identifiers: chr15:g.48738908C>A (hg19) ; chr15:g.48446711C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48446711C>A , CM000677.2:g.48446711C>A	GRCh38
NC_000015.9:g.48738908C>A , CM000677.1:g.48738908C>A	GRCh37
NC_000015.8:g.46526200C>A	NCBI36
NG_008805.2:g.204078G>T , LRG_778:g.204078G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5783G>T	ENSP00000453958.2:p.Cys1928Phe
ENST00000674301.2:c.5783G>T	ENSP00000501333.2:p.Cys1928Phe
ENST00000684448.1:n.4457G>T
ENST00000316623.10:c.5783G>T MANE Select	ENSP00000325527.5:p.Cys1928Phe
ENST00000674301.1:c.782G>T	ENSP00000501333.1:p.Cys261Phe
ENST00000316623.9:c.5783G>T	ENSP00000325527.5:p.Cys1928Phe
ENST00000537463.6:c.*1546G>T	ENSP00000440294.2:n.*1546G>T
ENST00000559133.5:c.1090G>T
NM_000138.4:c.5783G>T , LRG_778t1:c.5783G>T	NP_000129.3:p.Cys1928Phe
NM_000138.5:c.5783G>T MANE Select	NP_000129.3:p.Cys1928Phe